ライフサイエンスコーパス: MIP

1 MIP was synthesized using COC as a template molecule, et

2 MIP-1beta, granulocyte colony-stimulating factor (G-CSF)

3 MIP-based chemical sensors allow label-free detection an

4 MIP-template interaction is verified also by Fourier Tra

5 MIPs are a promising option for industrial packed and fl

6 MIPs have been intensively employed in classical solid-p

7 MIPs have been utilized as receptors in biosensing platf

8 MIPs have found use as sorbents in sample preparation at

9 MIPs were prepared with the templates D-glucuronic acid

10 MIPs were synthesized by bulk polymerization of melamine

11 MIPs were synthesized by bulk polymerization using metha

12 MIPs were synthesized under different polymerization pro

13 MIPs, implemented as a recognition element due to their

14 mmatory protein (MIP)-1alpha/CCL3 (P<0.001), MIP-1beta/CCL4, and vascular endothelial growth factor (

15 operating conditions (1.5 mL of 200 mg L(-1) MIP-coated QDs solution, pH 5.5, and 15 min before fluor

16 associated with reduced inflammation (MCP-1, MIP-2, TNF-alpha, IL-6 and CD68), decreased accumulation

17 (MCP-1 [monocyte chemoattractant protein 1], MIP-1alpha/beta [macrophage inflammatory protein 1alpha/

18 mmatory cytokine responses (e.g., IL-1alpha, MIP-1alpha, TNF, IL-6, and IL-8) as well as regulated a

19 cytokines (including chemokines MIP-1alpha, MIP-1beta, and IP-10).

20 P-1), macrophage inflammatory protein 1beta (MIP-1beta), and serum amyloid A protein (SAA) during acu

21 ttractant macrophage inflammatory protein-2 (MIP-2) and pulmonary neutrophil accumulation.

22 s such as macrophage inflammatory protein-2 (MIP-2), ILs, TNFalpha, and the effect was completely dim

23 ssion of chemokines/cytokines such as CCL-3 (MIP-1alpha) and granulocyte-macrophage colony-stimulatin

24 lpha)/CCL3 [chemokine (C-C motif) ligand 3], MIP-1beta/CCL4, RANTES (regulated on activation, normal

25 Further, a MIP based cartridge was designed to use in extraction pr

26 After MIP film deposition, the template was removed, and was c

27 The selectivity of the AMP-MIP was evaluated in presence of other structurally rela

28 of 2,3'-bithiophene enables deposition of an MIP film in the form of an inverse opal.

29 The specific binding of an MIP to a nonimprinted polymer (NIP) reached up to 560%.

30 removing template is evaluated by analyzing MIP films before and after the treatment by X-ray photoe

31 04), IL-6 (P = 0.001), IL-10 (P = 0.04), and MIP-2 (P = 0.02) expression, neutrophil (P = 0.02) and m

32 8/CXCL8 (P<0.001), MCP-3/CXCCL7 (P<0.05) and MIP-1alpha/CCL-3 (P<0.05) were significantly upregulated

33 On treatment, IP-10 and MIP-1beta levels were significantly higher in individual

34 ing cytokine secretion, especially IL-10 and MIP-1beta.

35 Interleukin (IL)-1beta, IL-6, IL-10, and MIP-2 were determined by Bio-Plex bead array.

36 tered neutrophil recruitment, MIP-1alpha and MIP-2 chemokine expression, and vascular endothelial gro

37 olony-stimulating factor [GM-CSF], IL-4, and MIP-1alpha) responses of the treated mice was observed,

38 f proinflammatory cytokines (IL-6, IL-8, and MIP-1beta) by monocytes and DCs (IC50 < 1 muM) and preve

39 ly decreased the production of TNF-alpha and MIP-2 in bronchoalveolar lavage fluid.

40 to syntheses of nanostructured MIP films and MIP nanoparticles.

41 It colocalized GABA and MIP but not AT or ORC immunoreactivity.

42 In contrast, when MIP-GlcA and MIP-NANA particles with a smaller size (125nm) were used

43 rituximab, rituximab-F(ab')2, or medium and MIP-1beta, IL-10, interferon-gamma, and tumor necrosis f

44 MIB and MIP are encoded by two genes organized in tandem, with h

45 highly selective aptamer-lined pockets (apta-MIP) with FETs for sensitive detection of prostate speci

46 The present apta-MIP sensor developed in conjunction with FET devices dem

47 dded aptamer to form a hybrid receptor (apta-MIP), displaying recognition properties superior to that

48 The apta-MIP sensor showed high sensitivity with a linear respons

49 uate subsequent rebinding of PSA to the apta-MIP surface.

50 developed more and more (enzymes, aptamers, MIPs); their advantages and drawbacks are discussed in t

51 ry information is directed to parietal areas MIP and LIP during decision formation.

52 ly, medial and anterior intraparietal areas (MIP and AIP), and parietal area PEip; somatosensory area

53 tion of the CC chemokine CCL3 (also known as MIP-1alpha), which recruits monocytes to the area in whi

54 were compared against commercially available MIPs according to specificity and selectivity metrics; c

55 be readily adapted to design other PDA-based MIP sensors.

56 thesis as well as for preparing the QD based MIP-coated composite by precipitation polymerization (im

57 The best MIP was morphologically characterized and equilibrium as

58 -1), macrophage inflammatory protein 1 beta (MIP-1beta), and interleukin-18 (IL-18) in 131 patients w

59 XPS) also evidencing the correlation between MIP chemical structure and its rebinding ability.

60 Both MIPs were found to be highly selective towards their tar

61 CXCL10 (IP-10), sIL-1RII, sIL-2RA, and CCL3 (MIP-1A) were strongly and significantly associated with

62 , we found a significant reduction in CD107a/MIP-1beta expression in HIV-1-specific CD8(+) T cells.

63 th selective ablation of GIPR in beta cells (MIP-Cre:Gipr(Flox/Flox); Gipr(-/-betaCell)) exhibit lowe

64 L-6, IL-1beta), neutrophil chemoattractants (MIP-2, KC), neutrophil infiltration (MPO activity), lipi

65 inflammatory cytokines (including chemokines MIP-1alpha, MIP-1beta, and IP-10).

66 developed microfluidic biochips with on-chip MIP biosensors present the advantages of a compact size,

67 cificity and selectivity metrics; commercial MIPs were characterized by quite broad cross-reactivity

68 Under the selected optimal conditions, MIP sensor shows a linear range from 0.15 to 3.7 mM SDM,

69 ts show that the response of PVA/MnO2@GO/CuO MIP is much higher than PVA/MnO2@GO/CuO non-imprinted el

70 The miRNA-induced cytokine (MIP-2, TNF-alpha, and IL-6) production was abolished in

71 atively regulates pro-inflammatory cytokines MIP-1alpha and IL-17A.

72 Such we obtained one D1R-MIP-QCM electrode, whereas the other electrode carried t

73 Our experiments revealed that D1R-MIP sensors are useful for estimating the strength of li

74 Sequencing results demonstrate MIPs capture and amplify targeted regions of interest at

75 e potential medical application of developed MIP sensors.

76 Finally, the developed MIP-voltammetry system was successfully applied for the

77 nted silica layers appended to quantum dots (MIP-QDs) with customized selective artificial recognitio

78 on, the use of ultrasound irradiation during MIP-QDs synthesis increased the homogeneity of the QDs s

79 absence of suspicious findings on the DWIBS MIPs.

80 s for facile integration of electrodeposited MIP film with FET transducer.

81 conventional infrared spectroscopy, our epi-MIP microscope enabled mapping of both active pharmaceut

82 epi-detected mid-infrared photothermal (epi-MIP) microscope at a spatial resolution of 0.65 mum.

83 best of our knowledge there are no existing MIPs-based sensors toward amphetamine-type stimulants (A

84 n with a molecularly imprinted polymer film (MIP), viz., myoglobin-imprinted electropolymerized poly(

85 y, each of the interferences with a "frozen" MIP-Nic molecular cavity.

86 otocin, RGWamide, DLamide, FLamide, FVamide, MIP, and serotonin were present in fewer cells in demarc

87 The expressed G212R-MIP was diminished and almost exclusively cytoplasmic in

88 ial overlap between areas of maximal MR(gluc)MIP and maximal TSCR was 29.5% +/- 5.1%.

89 of maximal uptake on PET/CT-derived MR(gluc)MIP images.

90 Glucose uptake on MR(gluc)MIP was found to correlate positively with a change in T

91 However, MIP-CreERT mice on different genetic backgrounds were pr

92 e PSMA inhibitors (123)I-MIP-1972 and (123)I-MIP-1095.

93 th the small-molecule PSMA inhibitors (123)I-MIP-1972 and (123)I-MIP-1095.

94 th (68)Ga-PSMA-11 for PET imaging and (131)I-MIP-1095 for endoradiotherapy of metastatic prostate can

95 imprinting factor determined as a ratio Imax(MIP)/Imax(NIP) of 2-4.

96 IL-8) or bridge innate to adaptive immunity (MIP-3alpha and RANTES (regulated on activation normal T

97 ve focused on the most promising advances in MIP-based biosensors to illustrate how close to market t

98 We observed an increase in MIP-1alpha (macrophage inflammatory protein-1alpha)/CCL3

99 of apoptotic cells compared to that seen in MIP-Cre controls.

100 ted RAW macrophages, both alarmins increased MIP-2 (macrophage inflammatory protein-2) chemokine expr

101 ion of TLR3 had no impact on the RNA-induced MIP-2 response.

102 e with conditional (betaraKO) and inducible (MIP-betaraKO(f/f)) raptor deletion.

103 al Impact Model Intercomparison Project (ISI-MIP, including HYBRID4, JeDi, JULES, LPJml, ORCHIDEE, SD

104 olated from beta-cell-specific Ghsr knockout MIP-Cre/ERT;Ghsr(f/f) mice.

105 uted 1:2 with PBS buffer was analyzed by LDL-MIP sensors to demonstrate applicability to real-life sa

106 The LDL-MIP sensor reveals analytical accuracy of 95-96% at the

107 The LSPR/MIP sensor provided a linear response for astringency ex

108 The capacity of Mag-MIP for biotin adsorption, its kinetics and selectivity

109 ied with molecularly imprinted polymers (Mag-MIP) through core-shell method for the determination of

110 ivity experiments revealed that prepared Mag-MIP had higher selectivity toward biotin compared to oth

111 The Mag-MIP and Mag-NIP were characterized by FTIR, magnetic hys

112 The magnetic-MIP showed a significant immobilization capacity of biot

113 The application of the magnetic-MIPs for the detection of biotin and biotinylated DNA in

114 Meanwhile, MIP-1404, PSMA-11, 2-(3-{1-carboxy-5-[(6-fluoro-pyridine

115 s prepared by a molecular imprinting method (MIP).

116 studies suggest that genes encoding the MIB-MIP system are specific to mycoplasmas and have been dis

117 pillary (PAP), acinar (ACN), micropapillary (MIP), or solid (SOL)-present in the tumor.

118 mainly antibodies to surface antigens (MOMP, MIP, Pmp13G), all of which did not persist.

119 a strong antibody response to surface (MOMP, MIP, Pmp13G) and virulence-associated (CPAF, TARP, SINC)

120 All images included axial, MPR, MIP, and VRT and were interpreted in one session.

121 otential (P, V), were measured for the MWCNT/MIP-sensors after their incubation with non-diluted plas

122 structures of reactive sites resulted in a N-MIP with excellent affinity to cTnT binding (KD=7.3 10(-

123 The analytical performance of cTnT N-MIP performed by differential pulse voltammetry showed a

124 A nano-molecularly imprinted polymer (N-MIP) assembled on a screen-printed electrode for the car

125 The N-MIP proposed is based on a simple method of antibody obt

126 has been paid to syntheses of nanostructured MIP films and MIP nanoparticles.

127 patients with bladder cancer using the NMP22 MIP-coated ZnO nanorods electrodes that were integrated

128 genetic and functional evidence for a novel MIP mutation of G212R, which leads to congenital progres

129 ted ADCC and antibody-mediated activation of MIP-1beta in NK cells as the four immunological paramete

130 is necessary for the proteolytic activity of MIP.

131 The binding affinity of MIP was calculated by static and kinetic adsorption stud

132 will discuss the current state-of-the-art of MIP synthesis and applications in the context of food an

133 This combination of MIP nanoparticles with micromechanical sensors is one of

134 w surveys novel achievements in the field of MIP nanostructures and their application for determinati

135 The fluorescence of MIP-coated QDs was quenched by the template (COC) and al

136 otein expression level of the mutant form of MIP was remarkably reduced compared with that of the wil

137 kely to damage the structure and function of MIP.

138 s synthesis and surface functionalization of MIP microspheres and nanoparticles are well established,

139 e CD4(+) T cells that produce high levels of MIP chemokines, which block R5-tropic HIV entry.

140 rollers, we observed increased production of MIP-1alpha and/or MIP-1beta at the protein level.

141 lective fluorescence quenching properties of MIP-QDs toward cypermethrin (CYP) are due to strong inte

142 ted QDs; and also, fluorescence quenching of MIP-coated QDs was not observed by other drugs of abuse

143 In the optimal condition, response of MIP sensor to mel was linearly proportional to its conce

144 , we developed a method for the synthesis of MIP nanoparticles (nanoMIPs) using an innovative solid-p

145 Novel techniques of MIP deposition as thin films, surface development, and i

146 After the best batch of MIPs was chosen, different strategies for immobilizing t

147 rent limitations in the commercialisation of MIPs technology.

148 To control the specificity of MIPs, a different antibiotic enrofloxacin (ENF), with a

149 rovide first evidence for the suitability of MIPs to selectively recover ribonucleoprotein complexes

150 The ELISA-like method based on MIP-QDs can be successfully employed to detect residual

151 of right and left breasts were evaluated on MIP and post-contrast T1-weighted magnetic resonance ima

152 of recovery of fenarimol was 91.16-99.52% on MIPs.

153 Two abbreviated protocols (APs) based on MIPs were evaluated regarding the potential to exclude m

154 -D) was applied to characterize and optimize MIP/NIP electrosynthesis.

155 ed increased production of MIP-1alpha and/or MIP-1beta at the protein level.

156 Surprisingly, two other MIPs are Mck1 and Mkk2 that are the upstream kinases of

157 e glycol dimethacrylate)] polymer particles (MIPs) for CO2 capture were synthesized by suspension pol

158 t-dispersing factor, myoinhibitory peptides (MIPs), and orcokinins (ORCs) were part of both entrainme

159 cularly imprinted and non-imprinted polymer (MIP and NIP) showed that MIP possesses a higher affinity

160 Molecular imprinted polymer (MIP) against cephalexin was synthesized by co-polymeriza

161 by the layer of molecular imprinted polymer (MIP) as the recognition medium.

162 is to develop molecularly imprinted polymer (MIP) based micromechanical cantilever sensor system that

163 osed that the molecularly imprinted polymer (MIP) cavity would act synergistically with the embedded

164 purified using molecular imprinted polymer (MIP) columns specifically designed for OTA.

165 the deposited molecularly imprinted polymer (MIP) film on three length scales.

166 tegrated with molecularly imprinted polymer (MIP) film recognition units.

167 The molecularly imprinted polymer (MIP) film showed an appreciable apparent imprinting fact

168 A molecularly imprinted polymer (MIP) for sulfamethizole (SMZ) selective recognition was

169 li-responsive molecularly imprinted polymer (MIP) for trace level sensing of alpha-fetoprotein (AFP),

170 onsisted of a molecularly imprinted polymer (MIP) layer for 8-OHdG assembled on a gold electrode thro

171 to prepare a molecularly imprinted polymer (MIP) layer on the surface of multi-walled carbon nanotub

172 molecule with molecularly imprinted polymer (MIP) layer results in the change in the dielectric natur

173 coated with a molecularly imprinted polymer (MIP) material selective toward cocaine and its metabolit

174 Molecularly imprinted polymer (MIP) nanoparticles including highly selective recognitio

175 ently-labeled molecularly imprinted polymer (MIP) particles for bioimaging of fixed and living human

176 osynthesis of molecularly imprinted polymer (MIP) templated with myoglobin (Mb) and the reference non

177 ) with embedded molecular imprinted polymer (MIP) to introduce selectivity for the di(2-ethylhexyl) p

178 ting from the molecularly imprinted polymer (MIP) was confirmed by the XPS analysis.

179 A new molecularly imprinted polymer (MIP)-based fluorescent artificial receptor has been prep

180 ctrogenerated molecularly imprinted polymer (MIP)-based ultrathin film using R(+)-atenolol (ATNL) as

181 rial based on molecularly imprinted polymer (MIP)-decorated magnetite nanoparticles for specific and

182 esized novel molecularly imprinted polymers (MIP) as biomimetic specific receptors to establish rapid

183 nce (LSPR) and molecular imprinted polymers (MIP) at gold nanodisks as an alternative to sensorial an

184 iterature on molecularly-imprinted polymers (MIPs) and some limited commercial activity, these promis

185 Molecularly imprinted polymers (MIPs) are artificial receptor ligands which can recogniz

186 Molecularly imprinted polymers (MIPs) are biomimetics which can selectively bind to anal

187 Molecularly imprinted polymers (MIPs) are synthetic materials, generally based on acryli

188 Molecularly imprinted polymers (MIPs) are tailor made recognition materials that can mim

189 nsor that uses molecular imprinted polymers (MIPs) coated with gold nanoparticles (GNPs) and reduced

190 A series of molecularly imprinted polymers (MIPs) comprising reactionary sites which are complementa

191 comprised of molecularly imprinted polymers (MIPs) for the specific recognition of NMP22 target molec

192 Molecularly imprinted polymers (MIPs) have been successfully applied as selective materi

193 decades now, molecularly imprinted polymers (MIPs) have successfully been used for selective chemical

194 electrode with molecular imprinted polymers (MIPs) immobilized on its surface.

195 onduction of molecularly imprinted polymers (MIPs) that employ label-free electrical detection techni

196 als", namely molecularly imprinted polymers (MIPs) to facilitate the isolation of ribosomes and trans

197 s to prepare molecularly imprinted polymers (MIPs) with ampicillin (AMP) and to evaluate the feasibil

198 We combine a molecularly imprinted polymers (MIPs) with surface enhanced Raman spectroscopy (SERS) to

199 particular, molecularly imprinted polymers (MIPs), by using the visible light emitted from QDs excit

200 In addition to sample preparation, MIPs have also been viewed as promising alternatives to

201 the fabrication of the sensor from prepared MIP nanocomposite.

202 The prepared MIP sensor is characterized by an apparent dissociation

203 The prepared MIP sensor was highly specific towards mel and the recog

204 single-stranded molecular inversion probes (MIPs) coupled to next-generation sequencing (NGS) for th

205 following the sad mood induction procedure (MIP).

206 PET/CT-derived maximum intensity projection (MIP) images from each subject, and the areas with the mo

207 he second component, Mycoplasma Ig protease (MIP), is a 97-kDa serine protease that is able to cleave

208 2 (P<0.05), macrophage inflammatory protein (MIP)-1alpha/CCL3 (P<0.001), MIP-1beta/CCL4, and vascular

209 t of the members of major intrinsic protein (MIP) family in controlling B transport.

210 used to identify Mst50-interacting proteins (MIPs) in this study.

211 d by mass spectrometry the performance of pY-MIP for enrichment and sequencing of phosphopeptides obt

212 The combination of pY-MIP- and TiO2-based phosphopeptide enrichment provided m

213 analysis of physicochemical properties of pY-MIP-TiO2-enriched phosphopeptides demonstrated that this

214 t using inexpensive pY-imprinted polymer (pY-MIP).

215 These unique properties render the pY-MIP-based phosphopeptide enrichment technique an attract

216 The pY-MIP-TiO2 and the TiO2 protocols yielded comparable numbe

217 ptides (approximately 70%) when using the pY-MIP-TiO2 combination as compared to TiO2 alone.

218 pY constituted up to 8% of the pY-MIP-TiO2-enriched phosphopeptide fractions.

219 r imaging with the two different colored QDs-MIPs was demonstrated.

220 tory markers including: MCP-1 SDF-1a, IL-Ra, MIP-1b, IL-8, and VEGF in comparison to unaffected child

221 More recently, MIPs have been combined with magnetic bead extraction, w

222 hamsters but altered neutrophil recruitment, MIP-1alpha and MIP-2 chemokine expression, and vascular

223 and the target was found, and a regenerative MIP-based virus detection assay was successfully develop

224 The stimuli-responsive MIP is composed of three components, a thermo-responsive

225 r has been prepared by anchoring a selective MIP for cocaine (COC) on the surface of polyethylene gly

226 Fluorescent sensory MIP (molecularly imprinted polymer) particles were combi

227 ion of molecular inversion probe sequencing (MIP-seq) and digital droplet PCR (ddPCR).

228 Several MIPs are conserved hypothetical proteins and may be invo

229 by integration of the fluorescent core-shell MIP sensor particles into a modular microfluidic platfor

230 The fabricated SMZ-MIP films were characterized in terms of their binding a

231 recise control of the thicknesses of the SMZ-MIP and respective nonimprinted reference films (NIP) wa

232 The SMZ-MIPs had SMZ binding capacity approximately more than ei

233 , low cost and highly sensitive CPX specific MIP nanoparticle based nanosensor developed in this rese

234 , a suitable platform to synthesize specific MIP cavities for Py and PLP.

235 crowave plasma-atomic emission spectrometry (MIP-AES).

236 Synthesized MIPs were packed into solid phase extraction (SPE) cartr

237 dsorption of thiabendazole using synthesized MIPs via precipitation polymerization.

238 (99m)Tc-trofolastat ((99m)Tc-MIP-1404), a small-molecule inhibitor of prostate-specif

239 Among them is (99m)Tc-MIP-1404, which has recently entered a phase 3 clinical

240 -imprinted polymer (MIP and NIP) showed that MIP possesses a higher affinity towards this analyte com

241 In addition, we show that MIPs can be used as an enrichment step with high resolut

242 Studies have consistently shown that MIPs can effectively minimize complex food matrix effect

243 The MIP film was prepared by electrochemical polymerization

244 The MIP films were synthesized and simultaneously deposited

245 The MIP is composed of a naphthalimide-based fluorescent mon

246 The MIP selectivity against low-(molecular weight) interfere

247 The MIP synthetic receptor was deposited by potentiodynamic

248 The MIP was evaluated as a sorbent for extraction and precon

249 The MIP with the highest binding capacity was selected.

250 The MIP/GNPs/rGO nano-hybrid film was immobilized onto a bar

251 optode containing the ion exchanger and the MIP particles (Miptode 2) showed improved selectivity ov

252 analyte which is selectively captured by the MIP onto the surface of the composite.

253 Following the MIP, there was a robust induction of depressed mood in t

254 of label-free responses originating from the MIP modified sensor.

255 imprinting, and then its releasing from the MIP was confirmed by the differential pulse voltammetry

256 (p.G212R) substitution was identified in the MIP gene through target region capture sequencing.

257 s achievements in recent developments of the MIP based e-tongues for chemosensing.

258 Integration of the MIP film as a recognition unit with a sensitive extended

259 The DPV and EIS response of the MIP film coated electrode to the HSA analyte was linear

260 AFM imaging of the MIP film surface indicated changes in mechanical propert

261 microgravimetric experiments with use of the MIP film-coated quartz crystal resonator, was found to b

262 Covalent and monolayer binding of the MIP nanoparticles on cantilevers was provided by EDC/NHS

263 , indicating the excellent efficiency of the MIP sites for target molecule recognition.

264 order to finely tune the performance of the MIP-based sensor.

265 The response of the MIP-CP electrode to fluoxetine was remarkably higher tha

266 istribution of the imprinted cavities on the MIP layer was confirmed by confocal microscopy imaging o

267 e resulted with 18.4-48.9pg mass load on the MIP modified cantilever.

268 rbent assay (ELISA)-like method based on the MIP-QDs was established under optimal conditions.

269 ites populated the imprinted cavities or the MIP surface only.

270 The results indicate that the MIP based AFM nanosensor has high sensitivity for the CP

271 The results demonstrated that the MIP/GNPs/rGO nano-hybrid film was suitable as the recogn

272 hesized via modified hummer's method, to the MIP-CP resulted in considerable enhancement in the sensi

273 unctionalising the gold sensor chip with the MIP nanoparticles using EDC/NHS coupling procedure.

274 The MIPs were synthesized by precipitation polymerization an

275 Importantly, the MIPs were not cytotoxic and did not affect cell viabilit

276 Two of the MIPs are Mst11 and Mst7 that are known to interact with

277 Characterization of the MIPs were carried out by Fourier-transform infrared spec

278 s with a smaller size (125nm) were used, the MIPs being synthesized as thin shells around green and r

279 system: first MIB captures the IgG, and then MIP is recruited to the MIB-IgG complex, enabling protea

280 cross-linker was co-polymerized into a thin MIP layer grafted from the surface of silica micropartic

281 This MIP was deposited as a thin film on an Au electrode by o

282 ndicate future possible applications of this MIPs-based capacitive biosensor for environmental and fo

283 As an alternative to MIP receptors, direct and sandwich assays were developed

284 tion of insulin sensitivity when compared to MIP-Cre controls.

285 ry neutrophil trafficking that is related to MIP-2 expression.

286 5-fold decrease in kidney uptake relative to MIP-1095.

287 ture langerin(high) MDLCs were responsive to MIP-3beta/CCL20 and CTAC/CCL27 chemokine stimulations.

288 combines the high selectivity attributed to MIPs and the sensitive fluorescent property of the Mn-do

289 as performed with trypsin-imprinted (trypsin-MIP) capacitive electrodes using standard trypsin soluti

290 The trypsin-MIP capacitive electrode was used for ~80 assays during

291 al from the mutant compared to the wild-type MIP.

292 p with an on-chip anesthetic biosensor using MIPs exhibited excellent performance in the separation a

293 ates, summarize the recent progress in using MIPs for preparing and analysing food samples, and discu

294 In contrast, when MIP-GlcA and MIP-NANA particles with a smaller size (125

295 One of the most interesting areas where MIPs have shown the biggest potential is food analysis.

296 The compounds were compared with MIP-1095, a PSMA ligand currently in clinical evaluation

297 keratinocytes with green QDs conjugated with MIP-GlcA and red QDs conjugated with MIP-NANA was demons

298 ed with MIP-GlcA and red QDs conjugated with MIP-NANA was demonstrated by fluorescence imaging.

299 increase the surface area to be coated with MIPs.

300 ytoplasmic in the HeLa cells; whereas the WT-MIP was stable dispersed throughout the cytoplasm, and i